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Pyridine → N-(t-butyloxycarbonyl)-4-(n-hexadecylamino)benzoyl-imidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | 4-(Hexadecylamino)benzoic acid | HCID 47263 | — |
| 反応物 | Carbonazidic acid, 1,1-dimethylethyl ester | HCID 61256 | — |
| 生成物 | N-(t-butyloxycarbonyl)-4-(n-hexadecylamino)benzoyl-imidazole | HCID 20437338 | — |
反応手順
A solution of 10 g. of 4-(n-hexadecylamino)benzoic acid in 100 ml. dioxane is treated with 4.0 g. of t-butylazidoformate and 10 ml. pyridine. After stirring at room temperature for 18 hours, the protected amido-acid is precipitated from solution by addition of 150 ml. of water. The product is collected and thoroughly dried. The crude product is dissolved in 200 ml. of a mixture consisting of methylene chloride/dimethoxy ethane/pyridine (1:4:1), and to this is added 5.4 g. of 1,1'-carbonyldiimidazoye. The solution is stirred overnight at room temperature and the solvents are evaporated to yield the title compound as a thick, orange oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04485105 |
| 出典データセット | uspto-grants-1984_11 |
| ORD ID | ord-b93f935ccbe942eeb013fcc325773199 |
| 出典メモ | uspto-grants-1984_11 |